Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene
Type 1 diabetes (T1D) is a complex autoimmune disease. Several genetic loci have been implicated in the susceptibility to this illness. Evaluated was the role of the CTLA4 exon 1 A49G polymorphism and its role as a risk factor for T1D in our population. DNA from 190 patients with T1D and their famil...
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Veröffentlicht in: | Human immunology 2004-07, Vol.65 (7), p.719-724 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Type 1 diabetes (T1D) is a complex autoimmune disease. Several genetic loci have been implicated in the susceptibility to this illness. Evaluated was the role of the CTLA4 exon 1 A49G polymorphism and its role as a risk factor for T1D in our population. DNA from 190 patients with T1D and their families and 96 control individuals were genotyped for CTLA4 exon 1 polymorphism and human leukocyte antigen (HLA)–DQB1*0201 and *0302 haplotypes by polymerase chain reaction (PCR) amplification–restriction enzyme analysis and PCR amplification that used sequence-specific primers, respectively. Patients were nonobese and |
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ISSN: | 0198-8859 1879-1166 |
DOI: | 10.1016/j.humimm.2004.04.007 |